The Chromosome 7 Annotation Project 

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#  Unique ID  Karyotype  Phenotype  Cytogenetic Break From  Cytogenetic Break To  Molecular Breakpoint #1  Molecular Breakpoint #2  Pubmed ID  Patient ID  Comments  

1  16317300_1  47, XY, upd(7) mat, +mar [9]. ish mar(7)(p11.2q11.21)(AC023141/ Q9BWX6/ D7S619+, D7Z1+, AC017075+)/ 46, XY, upd(7)mat [16]  pre & postnatal growth retardation, triangular face, relative macrocephaly, mild psychomotor retardation, ear anomalies, squeaky voice  some features of SilverRussell syndrome  p11.2  q11.21  D7S674/ AC023141  D7S2429/ D7S663  16317300  maker 7  paternal origin  Edit  
2  13680362_12  47, XX, +mar [10] de novo/ 46, XX [12] [amniocytes] 7p+; cep 7+ min(7)(:p11.2> q11.1:) [subcenMFISH]  phenotypically normal  p11.2  q11.2  16434320  Edit  
3  18852357_1  mos 47,XY,+r(7)(p11.2q11.21)[22]/4 6,XY,upd(7) mat  myoclonusdystonia syndrome, SilverRussell syndrome, intrauterine growth retardation, growth retardation, premature puberty, dystonia, myoclonus, small triangularshaped face, prominent forehead, hypertelorism, smallmouth with thin lips,micrognathia with pointed chin, low posteriorrotated andoverfolded ears  p11.2  q11.21  RP51091E12  RP11340I6  18852357  Edit  
4  Shimizu_A413  47, XX, +7p  dysmorphic face, congenital heart defects, arched eyebrows, hypertelorism, lowset and malformed ears, broad nose, micrognathia, highly arched palate, short and webbed neck, hip joint dislocation and overlapped fingers  pter  p10  Shimizu et al., abstract, A413  Edit  
5  6733951  47, XX, +7 [12%]/ 46, XX [88%]  Potter syndrome, pulmonary hypoplasia, renal agenesis, died 14 hrs after birth  pter  qter  6733951, 10594874, 12124684, 16092121  Edit  
6  8411076  47, XY, +7 [9] [amniotic fluid, 1st culture] 46, XY [30] [amniotic fluid, 2nd culture] 46, XY [60] [blood, aged 7] 47, XY, +7 [23]/ 46, XY [13] [skin, aged 8]  hypomelanosis of Ito, mild developmental delay, facial asymmetry, cleft uvula, enamel dysplasia  pter  qter  8411076, 9110367, 10594874, 16092121, 12124684, 16302164  VII4 [9110367]  Edit  
7  10594874_1  46, XY [293]/ 47, XY, +7 [56]/ 46, XY, r(7) [60]/ 47, XY, +7, r(7)[2]  intrauterine growth retardation, short stature, moderate mental retardation, multiple minor anomalies, pigmentation anomalies  pter  qter  10594874  Edit  
8  7390476  47, XX, +7 de novo  Potter syndrome, hypertelorism, depressed nasal bridge, lowset ears, micrognathia, short neck, narrow pelvis, bilateral clubfoot, hypotonicity, anal imperforation, abnormal external genitals, no opening to vagina, vertebral abnormalities, polycystic and hydronephrotic kidney, hypoplastic lungs  pter  qter  7390476, 6733951, 10594874, 12407716  twin brother had normal karyotype  Edit  
9  10594873  47, XY, +7 [28]/46, XY [7] [skin]  linear and whorled nevoid hypermelanosis, hypomelanosis of Ito, DandyWalker variant, developmental delay, hypotonia, pyschomotor delay, heart defect (PDA & VSD), asymmetric ptosis, short downslanting palpebral fissures, sparse eyelashes  pter  qter  10594873, 10594874  Edit  
10  Unpublished_54  46, XY, mar(7)  cognitive delay, emotional difficulties, mild dysmorphic features, multiple pigmented nevi  pter  qter  54  data unpublished  Edit  
11  7341641  47, XX, +7/ 46, XX [skinright forearm] 46, XX [blood, skinleft forearm]  plagiocephaly, abnormalities of left ear, facial asymmetry, abnormalities of head hair pattern, cleft lip and palate, bifid tongue, left torticollis, hemivertebrae, left radial hypoplasia and absent thumb, left inguinal hernia, patient ductus arteriosus, narrowing of the thoracic aorta, and hypoplastic right pulmonary artery  pter  qter  7341641, 10594874, 12124684, 16092121  Edit  
12  12128070  47, X?, +7  primary osteorarthritis of the knee/hip  pter  qter  12128070  synovial cells  Edit  
13  424118  47, XX, +7 de novo  phenotype not given  pter  qter  424118  trisomy due to nondisjunction of the second maternal meiotic division  Edit  
14  3812554  47, XY, +7 [42]/ 46, XY, +7 with random loss [3]/ 46, XY [11] [umbilical cord cells] 46, XY [21] [skin fibroblasts]  lowset ears, flattened face, renal dysplasia, pulmonary hypoplasia  pter  qter  3812554, 12124684, 12407716, 16092121  Edit  
15  1142382  47, XX +7 [14%]/ 46, XX [86%]  histeria  pter  qter  1142382, 10594874, 16092121  mother  daughter also had trisomy 7 mosaicism [9%]  Edit  
16  ECACC_92112305  48, XX, +7, +8  phenotype abnormal  pter  qter  92112305 (cell line: DD1078)  3rd consecutive miscarriage, IVF pregnancy; www.ecacc.or.uk  Edit  
17  ECACC_93080511  46, XX, mar(7)  developmental delay, autism  pter  qter  93080511 (cell line: CC0096)  www.ecacc.or.uk  Edit  
18  ECACC_95030626  46, XY/ 47, XY, +7  phenotypically normal  pter  qter  95030626 (cell line: DD2221)  fetus; chorionic villi sample for maternal age 43; 50% cells in this culture had +7; www.ecacc.or.uk  Edit  
19  NIGMS_GM03913  46, XY [46%]/ 47, XY, +7 [54%]  Roberts Syndrome (RBS)  pter  qter  GM03913  fibroblast, finite (primary) cell line from CCR: NIGMS Human Genetic Cell Repository  Edit  
20  NIGMS_GM09812  46, XX [92%]/ 47, XX, +7 [4%]/ 47, XX, +18 [4%]  qter  pter  GM09812  lymphoblast: 46,XX/47,XX,+ 12; fibroblast, finite (primary) cell line from CCR: NIGMS Human Genetic Cell Repository  Edit  
21  NIGMS_GM14084  45, XX, 3 [2]/ 45, XX, 17 [2]/ 45, XX, 22 [2]/ 46, XX [88]/ 47, XX, +7 [4]/ 47, XX, +8 [2]/ 47, XX, +14 [2]  severe microcephaly, developmental delay  pter  qter  GM14084  fibroblast, finite (primary) cell line from CCR: NIGMS Human Genetic Cell Repository  Edit  
22  1756501  48, XY, +7, +i(12)(p10) [24]  46,XY female, mixed gonadal dysgenesis teratoma (mature and immature) and yolk sac elements  pter  qter  1756501  Mitelman Database, Reference No. 4090  Edit  
23  8923948  47, X?, +7/ 46, X?  2 of 14 were small for gestational age; the rest were normal  pter  qter  8923948, 9106539  14 cases  14 pregnancies diagnosed by CVS; followup amniocentesis showed normal karyotype  Edit  
24  15337469_1  47, XX, +mar. ish r(7)(p?q?)(D7Z1+, ELN+) [38]/ r(7)(D7Z1++, ELN++) [2] de novo / 46, XX [12]  mild motor developmental delay, broad forehead, asymmetrical facial appearance, plagiocephaly, short nose with anteverted nostrils, long and slender extremities, moderate deafness  pter  q21.2  ELN/ D7S522  15337469  case 1  in 4% of the cells analyzed, maker r(7) was duplicated and dicentric (D7Z1, ELN)  Edit  
25  15337469_2  47, XY, +mar. ish r(p?q?)(D7Z1+, ELN+) [48]/ r(7)(D7Z1++, ELN++) [2] de novo / 46, XY [50]  borderline performance, obesity, hyperactivity with fits of anger, speech difficulties, hypertelorism, downslanting palpebral fissures, IQ of 80  pter  q11.2  15337469  case 2  in 2% of the cells analyzed, maker r(7) was duplicated and dicentric (D7Z1, ELN)  Edit  
26  von Beust_ESHG2004  47, XX, +mar [26]/ 46, XX [14] [marker was derived from chr. 7]  congenital heart defect, dysmorphic features  pter  qter  von Beust et al., ESHG 2004, P0172  Edit  
27  12605443  47, XX, +7 [13]/ 46, XX [19] [amniocytes] 47, XX, +7 [50] [cord blood] 47, XX, +7 [19] [postpartum chorionic villus] 47, XX, upd(7)mat, +7 [9]/ 46, XX, upd(7)mat [20] [skin] upd(7)mat [confirmed by microsatellite markers, peripheral blood]  posteriorrotated lowset ears, prominent forehead, small chin, triangular face, obstructed left nares, prominent nasal bridge, reversed epicanthal folds, thin lips, small mouth, micrognathia, bilateral clinodactyly of V finger, bridged Simian crease on left hand  pter  qter  12605443, 16007591, 16302164  trisomy 7 two maternal and one paternal chromosomes & maternal uniparental heterodisomy  Edit  
28  16092121  47, XX, +7 [12]/ 45, X [2]  hypopigmentation and hyperpigmentation following the Blaschko lines, growth retardation, buphthalmos of the left eye, mild mental retardation  pter  qter  16092121  Edit  
29  953215  47, XY, +C [possibly, +7]  flattened nasal bridge, posteriorly rotated lowset ears, prominent occiput, short neck, tapered fingers, clinodactyly of 5th dingers, bilateral diffuse renal dysplasia, pulmonary hypoplasia, died 17 hours after birth  pter  qter  953215, 6733951, 10594874  Trisomy 11 (+C) was suggested in the first paper [953215]  Edit  
30  5420797  47, X?, +C de novo [possibly, +7]  flattened nasal bridge, epicanthic folds, micrognathia, lowset ears, midline cleft palate, hyperextensible joints, bilateral hip dislocation, bilateral polycystic disease of the kidneys (type II), polycystic ovaries, died one hour after birth  pter  qter  5420797, 6733951, 10594874  Edit  
31  15953408  4647, X, +7, X [cp18] XXX (74%), X (13%), XXXX (3%), XX (10%) [amniotic fluid cell, by FISH] XXX (75%), X (11%), XXXX (6%), XX (8%) [cord blood, by FISH]  IUGR, severe oligohydramnios, dysmorphic features, abnormal external genitalia, Potter syndrome, mesomelic dysmorphism [indicated by Xray]  pter  qter  15953408  aborted fetus at 32nd week  Edit  
32  8411070  46, XX [lymphocytes & dark skin fibroblasts] 47, XY, +7/ 46, XX [light skin keratinocytes]  developmental delay, epilepsy severely visually impaired, minimal white streaks on the right flank, hip and leg  pter  qter  8411070, 16092121  Edit  
33  12124684  47, XY, +7 [7]/ 46, XY [2] [amniotic fluid, 16 wks' gestation] 46, XY [blood, 20 wks' gestation] 46, XY [blood, 3yr 6m] 47, XY, +7 [36]/ 46, XY [64] [pigmented skin, 3yr 6m] 47, XY, +7 [24]/ 46, XY [76] [hypopigmented skin, 3 yr 6m]  facial asymmetry, congenital ptosis of left eye, facial paresis on left side, short left palpebral fissure, hypotonic, hypopigmentation on trunk and limbs following Blaschko's lines, enamel dysplasia, lowset & posteriorly rotated ears, sparse hair, undescended testes  pter  qter  12124684, 16302164  proband  Edit  
34  11102936  47, XY, +7 [43%]/ 46, XY [57%] [skin] 47, XY, +7 [3%]/ 46, XY [97%] [skin, second culture] 46, XY [100%] [blood]  developmental delay, asymmetrical growth, mixed receptiveexpressive language disorder, Blaschkolinear skin pigmentary changes (hypo/hyperpigmentation), aggressive behaviour  pter  qter  11102936  JB  Edit  
35  9110367_VII1  47, XY, +7 [48%]/ 46, XY [amniocytes] 46, XY [60] [blood] 46, XY [10] [skin]  phenotypically normal at 4.5 years of age  pter  qter  9110367, 16302164  VII1, AF9640  Edit  
36  9110367_VII2  47, XY, +7 [36.6%]/ 46, XY [amniocytes] 46, XY [203] [cord blood] 46, XY [100] [blood] 47, XY, +7 [18]/ 46, XY [20] [foreskin]  phenotypically normal at 4 years of age  pter  qter  9110367, 16302164  VII2, A133691  Edit  
37  9110367_VII3  47, XX, +7 [5%]/ 46, XX [amniocytes] 46, XX [blood & placenta]  phenotypically normal at birth  pter  qter  9110367, 16302164  VII3  Edit  
38  9110367_VII5  47, XX, +7 [31.3%]/ 46, XX [amniocytes] 46, XY [30] [amniotic fluid] 46, XX [CVS]  phenotypically normal at birth  pter  qter  9110367, 16302164  VII5, case KW  Edit  
39  9110367_VII6  47, XX, +7 [26.7%]/ 46, XX [amniocytes]  phenotypically normal at birth  pter  qter  9110367, 16302164  VII6, case AA  Edit  
40  9110367_VII7  47, XY, +7 [15%]/ 46, XY [amniocytes] 46, XY [30] [cord blood]  phenotypically normal at 25 months of age  pter  qter  9110367, 16302164  VII7, 41023  Edit  
41  9110367_VII8  47, XY, +7 [40%]/ 46, XY [amniocytes]  phenotypically normal at 4 months of age  pter  qter  9110367, 16302164  VII8, A9428241  Edit  
42  9855612  48, XY, +4, +7 [20]  phenotype not given  mother had incomplete abortion at the gestational age was 8~9 weeks [detected ultrasound]  pter  qter  9855612  abortus  mother was 42 years old  Edit  
43  10213044  47, XY or XX, +7  phenotype not given; mother had spontaneous abortion  pter  qter  10213044  12 cases (T71 to 12)  maternal origin  9 cases, paternal origin  1 case, origin not determined  2 cases; meiotic trisomy  10 cases, mitotic trisomy(?)  2 cases  Edit  
44  9832040  47, XY or XX, +7  phenotype not given; mother had spontaneous abortion  pter  qter  9832040  15 cases  maternal origin  12 cases, paternal origin  2 cases, origin not determined  1 case; maternal meiotic trisomy  6 cases, mitotic trisomy(?)  8 cases, unknown  1 case  Edit  
45  9556035  47, XX, +7 [11]/ 46, XX [14] [CVS] 46, XX [21] [longterm culture] 46, XX [30] [amniotic fluid]  phenotype not given  pter  qter  9556035  case 2  Edit  
46  3399481  47, XX, +7 [CVS] 46, XX [amniotic fluid cels] 46, XX [12] [placenta, central] 47, XX, t(2;21)(p13;q22), +20 [12]/ 46, XX [30] [placenta, peripheral] 46, XX [100] [cord blood]  phenotypically normal at birth  pter  qter  3399481  Edit  
47  9483638  47, XY or XX, +7/ 46, XY or XX  phenotypically normal on birth  pter  qter  9483638  cases 5, 6, 8 10  % of trisomic cells ranged from 9 to 40%  Edit  
48  9439664_1  48, XXX, +7  phenotype not given; mother had spontaneous abortion  pter  qter  9439664  case 1  Edit  
49  9439664_21  48, XX, +7, +12 [22]/ 46, XX [2]  phenotype not given; mother had spontaneous abortion  pter  qter  9439664  case 21  Edit  
50  9316135  48, XX, +7, +20 [4]/ 46, XX [4] [amniotic fluid, 16 wks] 48, XX, +7, +20 [15] [amniotic fluid, 20 wks] 46, XX [20] [CVS, 20 wks] 46, XX [30] [blood & fibroblast at birth]  phenotypically normal  pter  qter  9316135  Edit  
51  8655147_1  47, XX, +7 [27%]/ 46, XX [CVS] 47, XX, +7 [037%]/ 46, XX [term placenta]  phenotypically normal, normal birth weight  pter  qter  8655147  case 1  Edit  
52  8655147_6  47, XX, +7 [17%]/ 46, XX [CVS] 47, XX, +7 [027%]/ 46, XX [term placenta]  phenotypically normal, normal birth weight  pter  qter  8655147  case 6  Edit  
53  11464246_MZ570  47, XX, +7. rev ish enh(7)  phenotype not given; mother had spontaneous abortion  pter  qter  11464246  MZ570  Edit  
54  11464246_MR120  47, XX, +7. rev ish enh(7)  phenotype not given; mother had spontaneous abortion  pter  qter  11464246  MR120  maternal origin  Edit  
55  11464246_MR137  47, XY, +7. rev ish enh(7)  phenotype not given; mother had spontaneous abortion  pter  qter  11464246  MR137  paternal origin  Edit  
56  16302164  47, XX, +7 [3]/ 46, XX [15] [amniocytes, 17 wks] 47, XX, +7 [3]/ 46, XX [22] [amniocytes, at 18 wks] 46, XX [40] [CVS, 18 wks] 46, XX [40] [cord blood, placenta, liver, lungs, skin]  phenotypically normal; pregnancy was terminated  pter  qter  16302164  Edit  
57  7316468  48, XY, +7, +10  phenotype not given; mother had spontaneous abortion  pter  qter  7316468  advanced maternal age  37 years old  Edit  
58  1804088  47, XY, +7 [3]/ 46, XY [5] [CVS] 47, XY, +7/ 46, XY & 47, XY, +7 [placenta] 46, XY [blood, at birth]  phenotypically normal  pter  qter  1804088  Edit  
59  8878279_33  47, XY, +7 [3]/ 46, XY [8] [cytotrophoblasts] 46, XY [fetal cells after abortion]  phenotype not given; pregnancy was terminated because of Xlinked disease  pter  qter  8878279  case 33  Edit  
60  8878279_101  47, XY, +7 [2]/ 46, XY [14] [cytotrophoblasts] 46, XY [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  8878279  case 101  Edit  
61  8878279_14  47, XY, +7 [3]/ 46, XY [12] [cytotrophoblasts] 46, XY [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  2803989, 8878279  case 14  Edit  
62  8878279_102  47, XY, +7 [13]/ 46, XY [4] [cytotrophoblasts] 46, XY [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  8878279  case 102  Edit  
63  8878279_73  47, XX, +7 [4]/ 46, XY [13] [cytotrophoblasts] 46, XX [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  8878279  case 73  Edit  
64  8878279_55  49, XY, +3, +4, +7 [2]/ 48, XY, +3, +7 [1]/ 46, XY [14] [cytotrophoblasts] 46, XY [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  8878279  case 55  Edit  
65  8878279_78  48, XY, +4, +7 [3]/ 47, XY, +4 [3]/ 46, XY [8] [cytotrophoblasts] 46, XY [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  8878279  case 78  Edit  
66  8878279_105  55, XYY, +2, +3, +5, +7, +8, +11, +15, +20 [6]/ 46, XY [16] [cytotrophoblasts] 46, XY [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  8878279  case 105  Edit  
67  8878279_13  50, XY, +2, +3, +7, +15 [5]/ 46, XY [28] [cytotrophoblasts] 46, XY [amniocytes]  phenotype not given; pregnancy was continued  pter  qter  2803989, 8878279  case 13  Edit  
68  2235900_1  46, XY [CVS, direct] 47, XY, +7 [34%]/ 46, XY [66%] [CVS, culture] 47, XY, +7 [placenta, culture]  fatal demise detected by ultrasound at 15.5 weeks of gestation  pter  qter  2235900  case 1 (206188)  Edit  
69  2235900_2  46, XY [CVS, direct] 47, XY, +7 [53%]/ 46, XY [47%] [CVS, culture] 47, XY, +7 [8%]/ 46, XY [92%] [placenta, culture] 46, XY [cord blood & skin]  phenotypically normal at birth  pter  qter  2235900  case 2 (209289)  Edit  
70  3799715  47, XX, +7 [34]/ 46, XX [28] [CVS] 46, XX [100] [skin & umbilical cord]  phenotype not given; pregnancy was terminated at 10 weeks of gestation  pter  qter  3799715  Edit  
71  3228150  47, XY +7 [12]/ 46, XY [30] [CVS, culture 1] 47, XY +7 [11]/ 46, XY [36] [CVS, culture 2] 47, XY +7 [6]/ 46, XY [55] [CVS, culture 3] 47, XY +7 [1]/ 46, XY [30] [CVS, culture 4] 46, XY [100%] [fatal blood & amniotic fluid culture at 19 wks]  phenotype not given  pter  qter  3228150  Edit  
72  6475960  52, XX, +2, +7, +8, +12, +13, +20/ 46, XX [clitoral mass] 46, XX [blood & ovary]  ambiguous genitalia, clitoral mass; otherwise phenotypically normal  pter  qter  647596  Edit  
73  655633  47, XY, +7  phenotype not given; mother had repeated spontaneous abortions  pter  qter  655633  1 of 234 spontaneous abortion cases had trisomy 7  Edit  
74  6331788  47, XY, +7 [100%]  several malformations including severe anomalies of the splenomesenteric vascular system, persistence of Mullerian ducts, major anomalies of the anterior chamber of eye, facial dysmorphism; died at 3 months after birth  pter  qter  6331788  patient 240578  Edit  
75  8125474_3  47, XX, +7 [5]/ 46, XX [45] [amnion]  phenotype not given  pter  qter  8125474  3  Edit  
76  7450760  48, XX, +7, +22  phenotype not given; mother had spontaneous abortion  pter  qter  7450760  spontaneous abortus  one of 447 spontaneous cases karyotyped  Edit  
77  3580545  48, XX, +2, +7  phenotype not given; mother had spontaneous abortion  pter  qter  3580545  spontaneous abortus  one of 460 early spontaneous cases karyotyped  Edit  
78  4063875  48, XXX, +7  phenotype not given; mother had spontaneous abortion  pter  qter  4063875, 9439664  spontaneous abortus  one of 215 spontaneous abortion cases karyotyped  Edit  
79  9483638_7  48, XY, +7, +9 [2]/ 46, XY [17] [CVS]  phenotypically normal on birth  pter  qter  9483638  case 7  Edit  
80  18352813  47~48,XX,+der(7)t(7;7)(p22;?),+ der(7)(7?::7p22→7q11:: 7?)[cp7]  papillary glioneuronal tumor  pter  qter  18352813  Edit  
81  18397339_SE11  47,XY [6(q13q15),+ 7 detected by microarray]  subependymoma tumor in fourth ventricle  pter  qter  18397339  SE11  Edit  
82  18587327_2  4?, X?,+7  adenoid cystic carcinoma  pter  qter  18587327  case 2  observed in 4 of 12 (33%) cases  Edit  
83  18587327_6  4?, X?,+7  adenoid cystic carcinoma  pter  qter  18587327  case 6  observed in 4 of 12 (33%) cases  Edit  
84  18587327_10  4?, X?,+7  adenoid cystic carcinoma  pter  qter  18587327  case 10  observed in 4 of 12 (33%) cases  Edit  
85  18587327_11  4?, X?,+7  adenoid cystic carcinoma  pter  qter  18587327  case 11  observed in 4 of 12 (33%) cases  Edit  
86  18587327_13  4?, X?,+7  mucoepidermoid carcinoma  pter  qter  18587327  case 13  observed in 2 of 12 (17%) cases  Edit  
87  18587327_23  4?, X?,+7  mucoepidermoid carcinoma  pter  qter  18587327  case 23  observed in 2 of 12 (17%) cases  Edit  
88  18452823_1  46, XY.nuc ish +7 [68%], +17 [76%]  type 1 papillary renal carcinoma  pter  qter  18452823  Patient 1  sibling of 18452823_2, mother also affected by PRC  Edit  
89  18452823_2  46, XY.nuc ish +7 [60%], +17 [66%], Y [80%]  type 1 papillary renal carcinoma  pter  qter  18452823  Patient 2  sibling of 18452823_1, mother also affected by PRC  Edit  
90  18795325  47,XY,+7  endstage kidney disease  pter  qter  18795325  observed in 6 of 11 cases  Edit  
91  18592004_132  4?,XY,+7 [detected by microarray]  renal cell carcinoma  pter  qter  18592004  Case 132  observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes  Edit  
92  18592004_135  4?,XY,+7 [detected by microarray]  renal cell carcinoma  pter  qter  18592004  Case 135  observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes  Edit  
93  18592004_139  4?,XY,+7 [detected by microarray]  renal cell carcinoma  pter  qter  18592004  Case 139  observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes  Edit  
94  18592004_154  4?,XY,+7 [detected by microarray]  renal cell carcinoma  pter  qter  18592004  Case 154  observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes  Edit  
95  18592004_163  4?,XY,+7 [detected by microarray]  renal cell carcinoma  pter  qter  18592004  Case 163  observed in 32% of cases, discussion of FZD9, MET, EPHA1 as candidate genes  Edit  
96  18779729_1  4?,XX,del(3)(p25p25)+7[65%],+ 17[47%]  renal cell carcinoma  pter  qter  18779729  Case 1  Edit  
97  18779729_3  4?,XX,+7[64%],+ 17[36%]  papillary renal cell carcinoma  pter  qter  18779729  Case 3  Edit  
98  18779729_4  4?,XY,Y[98%],+7[60%],+ 17[28%]  papillary renal cell carcinoma  pter  qter  18779729  Case 4  Edit  
99  18779729_5  4?,XY,Y[100%],+7[44%],+ 17[12%]  papillary renal cell carcinoma  pter  qter  18779729  Case 5  Edit  
100  18779729_6  4?,XX,+7[46%],+ 17[40%]  papillary renal cell carcinoma  pter  qter  18779729  Case 6  Edit  
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